Canonical Allele Identifier: PA2741997369
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2779779
ClinVar RCV Id: RCV003665331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Arg64His
CA4239706
NM_033507.3:c.191G>A